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Macroporous alumina- and titania-based catalyst for carbonyl sulfide hydrolysis at ambient temperature

机译:大孔氧化铝和二氧化钛基催化剂在环境温度下用于羰基硫的水解

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摘要

In this study prepared alumina and titania carbonyl sulfide hydrolysis catalysts with three dimensional ordered macroporous (3DOM) structure were prepared by colloidal crystal template method. The fresh and used catalysts were characterized by X-ray diffraction, scanning electron microscopy, nitrogen adsorption studies, CO2 temperature programmed desorption (CO2-TPD) and Fourier transform infrared spectroscopy. The hydrolysis performance of the catalysts and their resistances to oxygen poisoning were evaluated in a fixed bed reactor at room temperature.It was found that the hydrolysis activity of the catalysts was remarkably enhanced by introduction of 3DOM structure because the effective pulling out of the hydrolysis product H2S from the porous structure significantly inhibited the deposition of sulfur on the surface of the catalysts. Adding surfactant P123 during the preparation of the 3DOM alumina-based catalyst increased the hydrolysis activity by increasing the surface area of the catalysts. Compositing SiO2 with the 3DOM titania-based catalysts could increase the surface area as well as benefit the formation of 3DOM structure. The optimum content of SiO2 was 33 wt%, at which both catalyst performance and the amount of basic sites as measured by CO2-TPD were highest. The hydrolysis activity of the catalysts in the presence of oxygen showed that the oxygen toxicity resistance of the 3DOM titania-based catalysts were better than the 3DOM alumina-based catalysts. The most abundant sulfur specie deposited on the surface of the titania-based catalysts was elemental sulfur for the alumina-based catalysts it was sulfate species. Sulfate not only blocked the pores of the catalysts but also deactivated the catalysts seriously for its acidity.
机译:本研究采用胶体晶体模板法制备了具有三维有序大孔(3DOM)结构的氧化铝和二氧化钛羰基硫化物水解催化剂。通过X射线衍射,扫描电子显微镜,氮吸附研究,CO2程序升温脱附(CO2-TPD)和傅里叶变换红外光谱对新旧催化剂进行了表征。在室温下在固定床反应器中评估了催化剂的水解性能及其对氧气中毒的抵抗力。发现通过引入3DOM结构显着提高了催化剂的水解活性,因为可以有效地抽出水解产物多孔结构中的硫化氢显着抑制了硫在催化剂表面的沉积。在3DOM氧化铝基催化剂的制备过程中加入表面活性剂P123通过增加催化剂的表面积而增加了水解活性。将SiO2与3DOM二氧化钛基催化剂复合可以增加表面积,并有利于3DOM结构的形成。 SiO 2的最佳含量为33wt%,在该温度下,催化剂性能和通过CO2-TPD测量的碱性位点的量最高。催化剂在氧气存在下的水解活性表明,3DOM二氧化钛基催化剂的抗氧毒性性能优于3DOM氧化铝基催化剂。沉积在二氧化钛基催化剂表面的最丰富的硫物种是氧化铝基催化剂的元素硫,它是硫酸盐。硫酸盐不仅阻塞了催化剂的孔,而且由于其酸性而使催化剂严重失活。

著录项

  • 来源
    《Fuel 》 |2019年第15期| 277-284| 共8页
  • 作者单位

    Taiyuan Univ Technol Cofounded Shanxi Prov & Minist Sci & Technol Inst Chem Engn Coal State Key Lab Coal Sci & Technol West Yingze St 79 Taiyuan 030024 Shanxi Peoples R China;

    Dalian Univ Technol Sch Chem Engn State Key Lab Fine Chem Dalian 116024 Peoples R China;

    Univ Saskatchewan Dept Chem Engn Saskatoon SK S7N 5A9 Canada;

    Shanghai Polytech Univ Shanghai Collaborat Innovat Ctr WEEE Shanghai Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    3DOM; Carbonyl sulfide; Hydrolysis; Alumina; Titania;

    机译:3DOM;羰基硫;水解;氧化铝;泰坦尼亚号;

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